# Citieffe S.R.L.

- Location (FDA's records): Calderara Di Reno, IT
- FDA decisions: 11 (2012–2025): 11 510(k) clearances
- Names in FDA's records: Citieffe S.R.L. (8); Citieffe (3)
- Product codes: HSB (5), KTT (3), HRS (1), HWC (1), JDW (1)
- 510(k) review time since 2016: median 219 days, against 132 for FDA's reviews in the same codes and years (1 of 5 faster)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Pega Medical, Inc.: 1 (https://510kreport.com/company/pega-medical)

## Firms that cite its devices most
- Arrowhead De, LLC: 1 (https://510kreport.com/company/arrowhead)

## Its most-cited devices
- K150661: ST.A.R. 90 F4 External Fixation Screws With Hydroxyapatite (2015), cited by 1

## Recent decisions
- K250197: Estremo Fibular Nail (Oct 17, 2025)
- K183666: EBA One Nailing System (Nov 14, 2019)
- K181540: Estremo Citieffe Nailing System (Jan 16, 2019)
- K180150: PL8 Wrist Reconstruction Plate (Aug 2, 2018)
- K163323: Dolphix® External Fixation System MR Conditional (Mar 20, 2017)
- K150661: ST.A.R. 90 F4 External Fixation Screws With Hydroxyapatite (Jul 7, 2015)
- K132363: Dolphix External Fixation System (Jan 16, 2014)
- K131005: EBA2 Femoral Nailing System (Jun 25, 2013)

Source page: https://510kreport.com/company/citieffe